Capricor Therapeutics, Inc. is hiring: Manufacturing Associate in San Diego

Capricor Therapeutics, a publicly traded (NASDAQ: CAPR) biotechnology leader, is driven by a mission to develop groundbreaking biologics—focusing on cell and exosome-based therapies—to make a meaningful impact on patients’ lives, particularly for severe conditions like Duchenne muscular dystrophy with our lead therapy, deramiocel (CAP-1002). Our innovative work extends to our StealthX™ exosome platform, harnessing cutting-edge science to address unmet medical needs through precision-engineered solutions. At the heart of everything we do is a deep commitment to patient-centered innovation, fueled by strong academic partnerships and a passion for advancing healthcare. As a Manufacturing Associate I/II, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success. Responsibilities Perform routine manufacturing tasks, including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing Complete and ensure timely, accurate documentation in compliance with GMP standards across batch records, forms, and protocols Mentor fellow team members on cGMP documentation protocols to ensure the highest standards Plan, collect, analyze, and report on production data, maintaining comprehensive records and observations Author, revise, and maintain SOPs through Capricor’s document change system Oversee inventory, material transfers, and cleanroom procedures to support efficient GMP operations Prepare technical summaries, protocols, and reports to ensure full documentation of production activities Lead moderate-complexity CAPAs and assist with deviations and investigations to maintain quality assurance Take on special projects in manufacturing and development as required Requirements Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field 1-3 years of experience in a cGMP/cGTP manufacturing environment Solid laboratory experience in mammalian tissue culture, along with expertise in aseptic techniques Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries Strong organizational skills and acute attention to detail within a fast-paced, dynamic setting Basic molecular biology and flow cytometry skills are a plus Adaptability to work schedules that may include weekends or holidays as needed Why Capricor? Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough. Come Work With Us! At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us. #J-18808-Ljbffr